Suzuki-Miyaura cross coupling reaction

• Catalysts 2017, 7, 146-168. DOI
• Front. Chem. 2015, 3, 10-12. DOI
• Molecules 2015, 20, 4967-4997. DOI
• Curr. Org. Chem. 2014, 18, 3141-3148. DOI
• RSC Adv. 2014, 4, 46218-46223. DOI
• RSC Adv. 2014, 4, 18558-18594. DOI
• Tetrahedron Lett. 2013, 54, 3374-3377. DOI
• New J. Chem. 2013, 37, 1989-1995. DOI
• Catal. Commun. 2013, 32, 101-107. 
• Synthesis 2013, 45, 330-333. DOI
• Applied Catalysis A: General 2013, 450, 13-18. DOI
• Synthesis 2012, 44, 767-772. DOI
• Dalton Transactions 2011, 40, 3116-3121. DOI
• ChemSusChem 2010, 5, 502-522. DOI
  

...

....

Heck-Mizoroki cross coupling reaction

• RSC Adv. 2014, 4, 46926-46929. DOI

Metathesis

• Synthesis 2012, 44, 137-143. DOI
• Sc. China Chem. 2010, 53, 1932-1936. DOI
• Carbohydr. Res. 2010, 345, 324-329. DOI
• Synlett 2007, 11, 1703-1706. DOI
• Tetrahedron Lett. 2006, 47, 6221-6224. DOI

Skraup / Doebner-Miller reaction

• J. Flow Chem. 2016, 6, 80-85. DOI
• Catal. Today 2015, 255, 66-74. DOI
• RSC Adv. 2014, 4, 21456-21464. DOI
• Catal. Commun. 2014, 44, 15-18. DOI
  

Pinacol coupling reaction

• J. Org. Chem. 2016, 81, 11065-11071. DOI
• ACS Sustainable Chem. Eng. 2016, 4, 6996-7003. DOI
• J. Org. Chem. 2015, 80, 6375-6380. DOI
• RSC Adv. 2015, 5, 46026-46030. DOI
• ChemSusChem 2015, 8, 1664-1675. DOI
  

Other

• Sustainable Chem. Pharm. 2024, 42, 101793. DOI
  Eur. J. Org. Chem. 2017, 6, 1078-1085. DOI (sélectionner par Synfacts ref: Synfacts 2017, 13, 0553)
• ChemCatChem 2016, 8, 2321-2328. DOI
• Beilstein J. Org. Chem. 2011, 7, 1228-1233. DOI